(3-(N,N-Diethylsulfamoyl)-4 -fluorophenyl)boronic acid
98%
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This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly in the development of boron-containing molecules. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic compounds, including drugs and agrochemicals. Its boronic acid functional group enables efficient coupling with aryl halides, making it valuable in the production of biaryl structures. Additionally, it finds application in the preparation of potential therapeutic agents targeting various diseases, leveraging its fluorine and sulfonamide groups for enhanced biological activity and metabolic stability. Its role in medicinal chemistry is significant, particularly in the design of enzyme inhibitors and receptor modulators.
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